Skip to main content
. 2023 Aug 8;46(10):961–974. doi: 10.1007/s40264-023-01338-9

Table 2.

Severity grading of adverse events following mass IDA versus DA therapy for the control of lymphatic filariasis

Type of event IDA (n = 4868) DA (n = 2865)
Grade 1 (mild) Grade 2 (moderate) Grade 3 (severe) Grade 1 (mild) Grade 2 (moderate) Grade 3 (severe)
Fever 298 (92.3%) 23 (7.1%) 2 (0.6%) 218 (91.2%) 21 (8.8%)
Loss of appetite 327 (95.3%) 15 (4.4%) 1 (0.3%) 288 (92.3%) 24 (7.7%)
Dizziness 1341 (85.2%) 33 (13.5%) 1 (0.4%) 489 (88.9% 60 (10.9%) 1 (0.2%)
Confusion 251 (90.9%) 22 (8.0%) 3 (1.1%) 93 (94.9 %) 5 (5.1%)
Drowsiness 892 (91.2%) 83 (7.8%) 3 (0.3%) 222 (90.6%) 23 (9.4%)
Headache 435 (91.4%) 37 (7.8%) 4 (0.8%) 426 (80.4%) 97 (18.3%) 7 (1.3%)
Cough 79 (81.4%) 16 (16.5%) 2 (2.1%) 187 (89.9%) 21 (10.1%)
Difficulty breathing 483 (88.9%) 5 (9.3%) 1 (1.9%) 30 (81.1 %) 7 (18.9%)
Nausea 222 (91%) 21 (8.6%) 1 (0.4%) 163 (88.1%) 21 (11.4%) 1 (0.5%)
Vomiting 183 (96.3%) 7 (3.7%) 144 (82.3 %) 31 (17.7%)
Diarrhea 93 (92.1%) 8 (7.9%) 86 (83.5 %) 17 (16.5%)
Stomach pain 184 (86.8%) 26 (12.3%) 2 (0.9%) 156 (85.2 %) 27 (14.8%)
Total 4353 (89.4%) 489 (10.0%) 26 (0.5%) 2502 (87.3%) 354 (12.4%) 9 (0.3%)

DA diethylcarbamnzine + albendazole, IDA ivermectin + diethylcarbazine + albendazole